Cas 79283-16-2,[3,5-Dichloro-4-(3-dibutylamino-propoxy)-phenyl]-(2-ethyl-indolizin-3-yl)-methanone; compound with oxalic acid

79283-16-2

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Basic information

Product Name: [3,5-Dichloro-4-(3-dibutylamino-propoxy)-phenyl]-(2-ethyl-indolizin-3-yl)-methanone; compound with oxalic acid
Synonyms: [3,5-Dichloro-4-(3-dibutylamino-propoxy)-phenyl]-(2-ethyl-indolizin-3-yl)-methanone; compound with oxalic acid
CAS NO:79283-16-2
Molecular Formula:
Molecular Weight: 593.548
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: [3,5-Dichloro-4-(3-dibutylamino-propoxy)-phenyl]-(2-ethyl-indolizin-3-yl)-methanone; compound with oxalic acid(CAS DataBase Reference)
NIST Chemistry Reference: [3,5-Dichloro-4-(3-dibutylamino-propoxy)-phenyl]-(2-ethyl-indolizin-3-yl)-methanone; compound with oxalic acid(79283-16-2)
EPA Substance Registry System: [3,5-Dichloro-4-(3-dibutylamino-propoxy)-phenyl]-(2-ethyl-indolizin-3-yl)-methanone; compound with oxalic acid(79283-16-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 79283-16-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 79283-16-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,8 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79283-16:
(7*7)+(6*9)+(5*2)+(4*8)+(3*3)+(2*1)+(1*6)=162
162 % 10 = 2
So 79283-16-2 is a valid CAS Registry Number.

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79283-16-2Relevant academic research and scientific papers

Research in indolizines series. Influence of substitution in the neighbourhood of ether function in butoprozine series

Rosseels,Peiren,Inion,et al.

, p. 581 - 588 (2007/10/02)

The authors prepared 2-alkyl or 2-aryl-3-(4-dialkylaminopropoxy-benzoyl)-indolizines with mono- or di-substitution in the ortho positions of the ether function. The substituents may be halogen atoms or methyl or methoxy groups. The 2-alkyl derivatives mon

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